欧盟EMA药品数据库(European Medicines Agency Authorisation of Medicines DataBase)
商品名称Avzivi
适用类别Human
治疗领域Colorectal Neoplasms;Carcinoma, Non-Small-Cell Lung;Carcinoma, Renal Cell;Ovarian Neoplasms;Fallopian Tube Neoplasms;Peritoneal Neoplasms;Uterine Cervical Neoplasms
通用名/非专利名称bevacizumab
活性成分bevacizumab
产品号EMEA/H/C/005574
患者安全信息No
许可状态Authorised
ATC编码L01XC07
是否额外监管Yes
是否仿制药或hybrid药物No
是否生物类似药Yes
是否附条件批准No
是否特殊情形No
是否加速审评No
是否罕用药No
上市许可日期2024/07/26
上市许可开发者/申请人/持有人FGK Representative Service GmbH
人用药物治疗学分组Antineoplastic agents
兽用药物治疗学分组
审评意见日期2024/05/30
欧盟委员会决定日期2024/07/26
修订号
治疗适应症Treatment of metastatic carcinoma of the colon or rectum, metastatic breast cancer and recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer first-line treatment of patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer. first line treatment of patients with advanced and/or metastatic renal cell cancer.
适用物种
兽用药物ATC编码
首次发布日期2024/08/08
产品说明书https://www.ema.europa.eu/en/documents/product-information/avzivi-epar-product-information_en.pdf
公共评估报告https://www.ema.europa.eu/en/medicines/human/EPAR/avzivi
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